Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance.
- NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_assertion description "[This is the first report of the molecular basis of prothrombin deficiency in Indian patients and we suggest the eponym 'Prothrombin Vellore 1' for Ala362 --> Thr mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance.
- NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_assertion evidence source_evidence_literature NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance.
- NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_assertion SIO_000772 15892853 NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance.
- NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_assertion wasDerivedFrom befree-20150227 NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance.
- NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_assertion wasGeneratedBy ECO_0000203 NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance.